NDC 68788-8358 – Divalproex sodium
Divalproex Sodium 500 mg/1 · Tablet, Extended Release · Oral
Product NDC68788-8358
Product details
- Brand name
- Divalproex sodium
- Generic name
- Divalproex sodium
- Labeler
- Preferred Pharmaceuticals, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA209286
- Marketed since
- February 13, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Divalproex Sodium 500 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8358-3 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-3) | Feb 13, 2023 |
| 68788-8358-6 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-6) | Feb 13, 2023 |
| 68788-8358-9 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-9) | Feb 13, 2023 |
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